1,3-Dipolar cycloaddition of pyridinium ylides to nitrostilbenes: synthesis of 1,2-diarylindolizines vs 3,4-diarylisoxazoline N-oxides

1,3-Dipolar cycloaddition of pyridinium ylides to nitrostilbenes: synthesis of 1,2-diarylindolizines vs 3,4-diarylisoxazoline N-oxides Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2025, Volume: 74, Number: 10, Pages: 3095-3102 Pages count : 8 DOI: 10.1007/s11172-025-4789-x

Authors

Kuznetsov N.A. ^1,2 , Podpovetnyi K.Ye. ^1,2 , Bogomolova O.A. ^1,2 , Ushkarov V.I. ¹ , Samet A.V. ¹ , Semenov V.V. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
2	Dmitry Mendeleev University of Chemical Technology of Russia, 9 Miusskaya pl., 125047, Moscow, Russian Federation

An effect of the substituents in pyridinium ylides on oxidative 1,3-dipolar cycloaddition to nitrostilbenes, the scope and limitations of this transformation were studied. This reaction depending of the nature of the substituents gave either 1,2-diarylindolizines or 3,4-diarylisoxazoline N-oxides.

Kuznetsov N.A. , Podpovetnyi K.Y. , Bogomolova O.A. , Ushkarov V.I. , Samet A.V. , Semenov V.V.
1,3-Dipolar cycloaddition of pyridinium ylides to nitrostilbenes: synthesis of 1,2-diarylindolizines vs 3,4-diarylisoxazoline N-oxides
Russian Chemical Bulletin. 2025. V.74. N10. P.3095-3102. DOI: 10.1007/s11172-025-4789-x WOS Scopus OpenAlex

Web of science:	WOS:001618041200009
Scopus:	2-s2.0-105022416545
OpenAlex:	W7106027329

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